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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241693Generated: October 31, 2026

Sodium Azide → 3-(1-Methyl-1H-tetrazol-5-yl)-5-nitro-benzoic acid ethyl ester

https://huagongshe.com/reaction/241693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantSodium BicarbonateHCID 516892—
ReactantN-Methyl-5-nitro-isophthalamic acid ethyl esterHCID 47099901—
Solvent1,1-DichloroethaneHCID 6365—
Product3-(1-Methyl-1H-tetrazol-5-yl)-5-nitro-benzoic acid ethyl esterHCID 6673340159.1%

Reaction Steps

To a 2M solution of N-methyl-5-nitro-isophthalamic acid ethyl ester (10 g) in dichloroethane (200 ml) at −20° C. was added pre-cooled triflic anhydride (10 ml) dropwise. This was stirred for 30 min and then sodium azide (4.6 g) was added. This was allowed to warm to room temperature and stirred overnight. The reaction was neutralised with 5% NaHCO3(aq) solution and the organic and aqueous layers were separated and the organic layer dried and concentrated in vacuum. Flash chromatography (100:0 to 50:50 gradient cyclohexane:EtOAc) afforded the title compound (6.5 g). Rt=1.52 min (method D).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653075B2
Source datasetuspto-grants-2014_02
ORD IDord-27933febf35047eb8471652ea9fb3111
Source noteuspto-grants-2014_02